The HD-ZIP IV transcription factor GLABRA2 acts as an activator for proanthocyanidin biosynthesis in Medicago truncatula seed coat

被引:5
|
作者
Gu, Zhiqun [1 ]
Zhou, Xin [1 ]
Li, Shuangshuang [1 ]
Pang, Yongzhen [2 ]
Xu, Yiteng [1 ]
Zhang, Xue [1 ,3 ]
Zhang, Jing [1 ]
Jiang, Hongjiao [1 ]
Lu, Zhichao [1 ]
Wang, Hongfeng [1 ,4 ]
Han, Lu [1 ]
Bai, Shiqie [5 ]
Zhou, Chuanen [1 ]
机构
[1] Shandong Univ, Sch Life Sci, Key Lab Plant Dev & Environm Adaptat Biol, Minist Educ, Qingdao 266237, Peoples R China
[2] Chinese Acad Agr Sci, Inst Anim Sci, Beijing 100193, Peoples R China
[3] Shandong Univ, Adv Med Res Inst, Cheeloo Coll Med, Jinan 250012, Peoples R China
[4] Shandong Peanut Res Inst, Qingdao 266199, Peoples R China
[5] Southwest Univ Sci & Technol, Sch Life Sci & Engn, Mianyang 621010, Peoples R China
基金
中国国家自然科学基金;
关键词
anthocyanidin reductase; HD-ZIP IV transcription factor; GLABRA2; Medicago truncatula; proanthocyanidin; seed coat; FLAVONOID BIOSYNTHESIS; ACCUMULATING CELLS; NEGATIVE REGULATOR; ANTHOCYANIN; PATHWAY; MUTANT; GENES; GLUCOSYLTRANSFERASE; DIFFERENTIATION; IDENTIFICATION;
D O I
10.1111/tpj.16918
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Proanthocyanidins (PAs), a group of flavonoids, are found in leaves, flowers, fruits, and seed coats of many plant species. PAs are primarily composed of epicatechin units in the seed coats of the model legume species, Medicago truncatula. It can be synthesized from two separate pathways, the leucoanthocyanidin reductase (MtLAR) pathway and the anthocyanidin synthase (MtANS) pathway, which produce epicatechin through anthocyanidin reductase (MtANR). These pathways are mainly controlled by the MYB-bHLH-WD40 (MBW) ternary complex. Here, we characterize a class IV homeodomain-leucine zipper (HD-ZIP IV) transcription factor, GLABRA2 (MtGL2), which contributes to PA biosynthesis in the seed coat of M. truncatula. Null mutation of MtGL2 results in dark brown seed coat, which is accompanied by reduced PAs accumulation and increased anthocyanins content. The MtGL2 gene is predominantly expressed in the seed coat during the early stages of seed development. Genetic and molecular analyses indicate that MtGL2 positively regulates PA biosynthesis by directly activating the expression of MtANR. Additionally, our results show that MtGL2 is strongly induced by the MBW activator complexes that are involved in PA biosynthesis. Taken together, our results suggest that MtGL2 acts as a novel positive regulator in PA biosynthesis, expanding the regulatory network and providing insights for genetic engineering of PA production.
引用
收藏
页码:2303 / 2315
页数:13
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